Variant report

Variant	esv1848387
Chromosome Location	chr11:76243699-76262652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:121)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:121 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:76246656-76246827	A549	lung:	n/a	n/a
2	CTCF	chr11:76262580-76262730	NHDF-neo	bronchial:	n/a	n/a
3	CTCF	chr11:76262580-76262730	AG04450	lung:	n/a	n/a
4	CTCF	chr11:76262560-76262710	AG09309	skin:	n/a	n/a
5	CTCF	chr11:76262500-76262650	AG04450	lung:	n/a	n/a
6	CTCF	chr11:76262560-76262710	HEEpiC	esophagus:	n/a	n/a
7	CTCF	chr11:76262600-76262750	NHEK	skin:	n/a	n/a
8	CTCF	chr11:76262600-76262750	AG04449	skin:	n/a	n/a
9	CTCF	chr11:76262620-76262770	HVMF	connective:	n/a	n/a
10	CTCF	chr11:76262560-76262710	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr11:76262640-76262790	RPTEC	kidney:	n/a	n/a
12	CTCF	chr11:76262560-76262710	AG04449	skin:	n/a	n/a
13	CTCF	chr11:76262540-76262690	HCM	heart:	n/a	n/a
14	CTCF	chr11:76262540-76262690	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr11:76262525-76262818	A549	lung:	n/a	n/a
16	CTCF	chr11:76262580-76262730	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr11:76262583-76262750	LNCaP	prostate:	n/a	n/a
18	CTCF	chr11:76262619-76262697	GM13977	blood:	n/a	n/a
19	CTCF	chr11:76262550-76262724	MCF-7	breast:	n/a	n/a
20	CTCF	chr11:76262540-76262690	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr11:76262620-76262770	BJ	skin:	n/a	n/a
22	CTCF	chr11:76262540-76262690	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr11:76262546-76262764	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr11:76262600-76262750	BJ	skin:	n/a	n/a
25	CTCF	chr11:76262520-76262670	HPF	lung:	n/a	n/a
26	CTCF	chr11:76262280-76262430	HCFaa	heart:	n/a	n/a
27	CTCF	chr11:76262580-76262730	AG09319	gingival:	n/a	n/a
28	CTCF	chr11:76262560-76262710	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr11:76262640-76262790	HMEC	breast:	n/a	n/a
30	CTCF	chr11:76262580-76262730	BE2_C	brain:	n/a	n/a
31	CTCF	chr11:76262560-76262710	HCT-116	colon:	n/a	n/a
32	CTCF	chr11:76262596-76262720	K562	blood:	n/a	n/a
33	CTCF	chr11:76262583-76262701	MCF-7	breast:	n/a	n/a
34	CTCF	chr11:76262560-76262710	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr11:76262515-76262798	A549	lung:	n/a	n/a
36	CTCF	chr11:76262572-76262688	Gliobla	brain:	n/a	n/a
37	CTCF	chr11:76262620-76262770	BE2_C	brain:	n/a	n/a
38	CTCF	chr11:76262540-76262690	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr11:76262600-76262750	HMF	breast:	n/a	n/a
40	CTCF	chr11:76262515-76262824	GM12878	blood:	n/a	n/a
41	CTCF	chr11:76262490-76262916	MCF-7	breast:	n/a	n/a
42	CTCF	chr11:76262634-76262713	Lung_OC	lung:	n/a	n/a
43	CTCF	chr11:76262501-76262819	IMR90	lung:	n/a	n/a
44	CTCF	chr11:76262598-76262731	LNCaP	prostate:	n/a	n/a
45	CTCF	chr11:76262498-76262811	K562	blood:	n/a	n/a
46	CTCF	chr11:76262560-76262710	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr11:76262580-76262730	AG10803	skin:	n/a	n/a
48	CTCF	chr11:76262560-76262710	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr11:76262480-76262630	NHLF	lung:	n/a	n/a
50	CTCF	chr11:76262560-76262710	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76261997-76262047	AG09319	gingival:	n/a
2	chr11:76261997-76262047	HEK293	kidney:	embryo
3	chr11:76261997-76262047	U87	brain:	n/a
4	chr11:76261997-76262047	GM12892	blood:	n/a
5	chr11:76261997-76262047	AG04450	lung:	fetal
6	chr11:76261997-76262047	MCF10A-Er-Src	breast:	n/a
7	chr11:76261997-76262047	H1-hESC	embryonic stem cell:	embryo
8	chr11:76261997-76262047	AG04449	skin:	fetal
9	chr11:76261997-76262047	BJ	skin:	n/a
10	chr11:76261997-76262047	LNCaP	prostate:	n/a
11	chr11:76261997-76262047	SAEC	small airway:	n/a
12	chr11:76261997-76262047	AoSMC	blood vessel:	n/a
13	chr11:76261997-76262047	BE2_C	brain:	n/a
14	chr11:76261997-76262047	PrEC	prostate:	n/a
15	chr11:76261997-76262047	SK-N-SH_RA	brain:	n/a
16	chr11:76261997-76262047	SKMC	muscle:	n/a
17	chr11:76261997-76262047	HCF	heart:	n/a
18	chr11:76261997-76262047	GM19239	blood:	n/a
19	chr11:76261997-76262047	ECC-1	luminal epithelium:	n/a
20	chr11:76261997-76262047	IMR90	lung:	fetal
21	chr11:76261997-76262047	PFSK-1	brain:	n/a
22	chr11:76261997-76262047	CMK	blood:	n/a
23	chr11:76261997-76262047	Hepatocyte	liver:	n/a
24	chr11:76261997-76262047	Jurkat	blood:	n/a
25	chr11:76261997-76262047	HUVEC	blood vessel:	n/a
26	chr11:76261997-76262047	NB4	blood:	n/a
27	chr11:76261997-76262047	GM06990	blood:	n/a
28	chr11:76261997-76262047	HMEC	breast:	n/a
29	chr11:76261997-76262047	HRE	kidney:	n/a
30	chr11:76261997-76262047	NT2-D1	testis:	n/a
31	chr11:76261997-76262047	HIPEpiC	eye:	n/a
32	chr11:76261997-76262047	HAEpiC	amniotic membrane:	n/a
33	chr11:76261997-76262047	HCPEpiC	choroid plexus:	n/a
34	chr11:76261997-76262047	HCT-116	colon:	n/a
35	chr11:76261997-76262047	HRCEpiC	kidney:	n/a
36	chr11:76261997-76262047	AG10803	skin:	n/a
37	chr11:76261997-76262047	HCM	heart:	n/a
38	chr11:76261997-76262047	A549	lung:	n/a
39	chr11:76261997-76262047	MCF-7	breast:	n/a
40	chr11:76261997-76262047	HRPEpiC	eye:	n/a
41	chr11:76261997-76262047	RPTEC	kidney:	n/a
42	chr11:76261997-76262047	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:76261997-76262047	K562	blood:	n/a
44	chr11:76261997-76262047	SK-N-MC	brain:	n/a
45	chr11:76261997-76262047	ovcar-3	ovarian:	n/a
46	chr11:76261997-76262047	NHBE	bronchial:	n/a
47	chr11:76261997-76262047	NHDF-neo	bronchial:	n/a
48	chr11:76261997-76262047	Hela-S3	cervix:	n/a
49	chr11:76261997-76262047	HEEpiC	esophagus:	n/a
50	chr11:76261997-76262047	HepG2	liver:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:76250200..76253023-chr11:76260666..76263366,2	K562	blood:
2	chr11:76250200..76253023-chr11:76260666..76263366,2	K562	blood:
3	chr11:76154176..76155961-chr11:76245444..76247160,2	K562	blood:
4	chr11:76261079..76263436-chr11:76264364..76265867,2	K562	blood:
5	chr11:76262380..76263432-chr11:76391914..76393026,4	MCF-7	breast:
6	chr11:76262469..76263152-chr11:76392001..76392517,2	K562	blood:
7	chr11:76243013..76244594-chr11:76251673..76254589,2	K562	blood:
8	chr11:76242469..76244011-chr11:76244453..76247142,2	MCF-7	breast:
9	chr11:76242469..76244011-chr11:76244453..76247142,2	MCF-7	breast:
10	chr11:76262034..76262940-chr11:76309241..76310049,2	K562	blood:
11	chr11:76246600..76249181-chr11:76252409..76254932,3	K562	blood:

No data

Variant related genes	Relation type
C11orf30	TF binding region
C11orf30	CpG island
ENSG00000158636	chromatin interactions
ENSG00000255135	chromatin interactions

Extended variants
information (count: 613 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1939467	chr11:76243699-76243700	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570321958	chr11:76243711-76243712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs544007525	chr11:76243715-76243716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563855870	chr11:76243733-76243734	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534666201	chr11:76243771-76243772	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529435567	chr11:76243800-76243801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149877263	chr11:76243848-76243849	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs370432496	chr11:76243854-76243855	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559828012	chr11:76243870-76243871	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2508756	chr11:76243901-76243902	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs551439662	chr11:76244011-76244012	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149313311	chr11:76244012-76244013	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs77992724	chr11:76244049-76244050	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533046591	chr11:76244053-76244054	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549986050	chr11:76244112-76244113	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569494935	chr11:76244118-76244119	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567029207	chr11:76244138-76244139	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147569472	chr11:76244171-76244172	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs78266341	chr11:76244177-76244178	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191124888	chr11:76244181-76244182	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116384380	chr11:76244183-76244184	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs557431447	chr11:76244232-76244233	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs578222610	chr11:76244327-76244328	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543736095	chr11:76244351-76244352	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183436170	chr11:76244360-76244361	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs574274404	chr11:76244422-76244423	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187588359	chr11:76244442-76244443	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544938798	chr11:76244461-76244462	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2513514	chr11:76244493-76244494	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs200445616	chr11:76244494-76244495	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201197504	chr11:76244521-76244522	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs559891243	chr11:76244532-76244533	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528550394	chr11:76244594-76244595	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs192534261	chr11:76244623-76244624	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73495416	chr11:76244639-76244640	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs376392340	chr11:76244661-76244662	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75791171	chr11:76244714-76244715	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569557462	chr11:76244730-76244731	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182233638	chr11:76244745-76244746	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548738141	chr11:76244755-76244756	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142046280	chr11:76244794-76244795	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534402993	chr11:76244798-76244799	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187614847	chr11:76244828-76244829	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551384618	chr11:76244848-76244849	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571151006	chr11:76244872-76244873	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537788570	chr11:76244874-76244875	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75069289	chr11:76244896-76244897	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574339711	chr11:76244955-76244956	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371762253	chr11:76244973-76244974	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192616983	chr11:76245015-76245016	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76205200-76254400	Weak transcription	Aorta	Aorta
2	chr11:76205400-76254600	Weak transcription	Right Ventricle	heart
3	chr11:76205400-76255200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:76206000-76249200	Weak transcription	Colonic Mucosa	Colon
5	chr11:76207400-76254400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:76213000-76254200	Weak transcription	Fetal Heart	heart
7	chr11:76220000-76255600	Weak transcription	Small Intestine	intestine
8	chr11:76222200-76252800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr11:76222600-76249200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:76224200-76254600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr11:76224400-76262600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:76224400-76263800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:76224800-76251200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:76225400-76253200	Weak transcription	HSMMtube	muscle
15	chr11:76230000-76265600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:76232800-76245000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr11:76233000-76249200	Weak transcription	Fetal Stomach	stomach
18	chr11:76233600-76251000	Strong transcription	Primary B cells from cord blood	blood
19	chr11:76233600-76258800	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr11:76233800-76258600	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr11:76233800-76260200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:76233800-76262000	Strong transcription	Placenta	Placenta
23	chr11:76233800-76262400	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr11:76233800-76262600	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr11:76233800-76263200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr11:76234000-76245200	Strong transcription	Fetal Thymus	thymus
27	chr11:76234000-76245400	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr11:76234000-76262600	Strong transcription	Dnd41	blood
29	chr11:76234200-76250800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr11:76234200-76251200	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr11:76234200-76262000	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr11:76234600-76246400	Weak transcription	Fetal Brain Male	brain
33	chr11:76234800-76263000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr11:76236000-76247400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr11:76236000-76254400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr11:76236000-76254400	Weak transcription	Gastric	stomach
37	chr11:76236200-76248800	Weak transcription	Ovary	ovary
38	chr11:76236200-76249200	Weak transcription	Fetal Intestine Small	intestine
39	chr11:76236200-76249200	Weak transcription	Lung	lung
40	chr11:76236200-76249400	Weak transcription	Spleen	Spleen
41	chr11:76236200-76253200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr11:76236200-76254400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr11:76236200-76254400	Weak transcription	Pancreas	Pancrea
44	chr11:76236400-76243800	Weak transcription	K562	blood
45	chr11:76236400-76245000	Weak transcription	NHLF	lung
46	chr11:76236400-76248800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr11:76236400-76250600	Weak transcription	Thymus	Thymus
48	chr11:76236400-76252600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr11:76236400-76255400	Weak transcription	HMEC	breast
50	chr11:76236400-76255600	Weak transcription	Esophagus	oesophagus

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